Renal Disease: Focal Segmental Glomerulonephritis Syndrome (FSGS) and membranous nephropathies
| Test Information | |
|---|---|
| Test Name | Renal Disease: Focal Segmental Glomerulonephritis Syndrome (FSGS) and membranous nephropathies |
| Lab (Location) | The Hospital for Sick Children |
| Category | Renal |
| Subcategory | Focal Segmental Glomerulonephritis Syndrome (FSGS) |
| Gene/Platform/Region List | ACTN4, ADCK4, CD2AP, COQ2, INF2, LAMB2, LMX1B, MYH9, NPHS1, NPHS2, PDSS2, PLCE1, SCARB2, SMARCAL1, TRPC6, WT1 |
| Test type | Gene Panel |
| Samples Accepted | Blood, DNA |
| Indications Diagnosis | Diagnosis, Prenatal |
| Test Methodology | Sequencing |
| Methodology Notes | Exome, Panel |
| Diseases/Conditions | Congenital Nephrotic Syndrome; Congenital Finnish Nephosis, Focal Segmental Glomerulosclerosis |